A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105149



Internal ID21498858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36661642..36661642hg38UCSC Ensembl
chr19:37152544..37152544hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383153
hg193153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654519
Supporting Variants
SamplesNA19239
Known GenesZNF461
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105149
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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